Variant report

Variant	esv2422250
Chromosome Location	chr13:85718435-85971539
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:85947684-85947808	HepG2	liver:	n/a	n/a
2	BACH1	chr13:85810629-85810724	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:85853164-85853173	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr13:85933207-85933215	GM12878	blood:	n/a	n/a
5	BRCA1	chr13:85770818-85770915	GM12878	blood:	n/a	n/a
6	CEBPB	chr13:85869191-85869393	HepG2	liver:	n/a	chr13:85869291-85869302 chr13:85869289-85869300 chr13:85869289-85869302
7	CEBPB	chr13:85858603-85858928	IMR90	lung:	n/a	chr13:85858748-85858757 chr13:85858748-85858757 chr13:85858746-85858759 chr13:85858746-85858759 chr13:85858748-85858759 chr13:85858748-85858759 chr13:85858748-85858757 chr13:85858748-85858757 chr13:85858746-85858759
8	CEBPB	chr13:85790608-85790853	HepG2	liver:	n/a	chr13:85790724-85790735
9	CEBPB	chr13:85892817-85892995	HepG2	liver:	n/a	chr13:85892866-85892877
10	CEBPB	chr13:85855330-85855670	IMR90	lung:	n/a	chr13:85855499-85855508 chr13:85855499-85855508 chr13:85855499-85855508
11	CEBPB	chr13:85927994-85928181	HepG2	liver:	n/a	chr13:85928083-85928092 chr13:85928083-85928094 chr13:85928083-85928092 chr13:85928081-85928094 chr13:85928081-85928094 chr13:85928083-85928092 chr13:85928081-85928094 chr13:85928083-85928092 chr13:85928081-85928092 chr13:85928083-85928094
12	CEBPB	chr13:85802863-85803190	Hela-S3	cervix:	n/a	chr13:85803034-85803045
13	CEBPB	chr13:85743470-85743533	HepG2	liver:	n/a	n/a
14	CEBPB	chr13:85802791-85803234	A549	lung:	n/a	chr13:85803034-85803045
15	CEBPB	chr13:85802861-85803189	K562	blood:	n/a	chr13:85803034-85803045
16	CEBPB	chr13:85810385-85810992	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr13:85810551-85810799	A549	lung:	n/a	n/a
18	CEBPB	chr13:85798053-85798369	IMR90	lung:	n/a	chr13:85798342-85798355
19	CEBPB	chr13:85802834-85803223	IMR90	lung:	n/a	chr13:85803034-85803045
20	CEBPB	chr13:85810442-85810983	A549	lung:	n/a	n/a
21	CEBPB	chr13:85815221-85815628	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr13:85787550-85787787	HepG2	liver:	n/a	chr13:85787640-85787653 chr13:85787714-85787725 chr13:85787640-85787651
23	CEBPB	chr13:85802858-85803211	H1-hESC	embryonic stem cell:	n/a	chr13:85803034-85803045
24	CEBPB	chr13:85855342-85855586	H1-hESC	embryonic stem cell:	n/a	chr13:85855499-85855508 chr13:85855499-85855508 chr13:85855499-85855508
25	CEBPB	chr13:85855338-85855651	HepG2	liver:	n/a	chr13:85855499-85855508 chr13:85855499-85855508 chr13:85855499-85855508
26	CEBPB	chr13:85866108-85866245	HepG2	liver:	n/a	chr13:85866196-85866207
27	CEBPB	chr13:85855327-85855634	A549	lung:	n/a	chr13:85855499-85855508 chr13:85855499-85855508 chr13:85855499-85855508
28	CEBPB	chr13:85903432-85903667	HepG2	liver:	n/a	chr13:85903579-85903590
29	CEBPB	chr13:85802799-85803218	HepG2	liver:	n/a	chr13:85803034-85803045
30	CHD2	chr13:85810575-85811051	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr13:85815267-85815546	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr13:85835880-85836030	GM12873	blood:	n/a	n/a
33	CTCF	chr13:85836040-85836190	MCF-7	breast:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
34	CTCF	chr13:85841687-85841738	LNCaP	prostate:	n/a	n/a
35	CTCF	chr13:85836064-85836168	MCF-7	breast:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
36	CTCF	chr13:85922000-85922150	AG10803	skin:	n/a	n/a
37	CTCF	chr13:85836020-85836170	AG09319	gingival:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
38	CTCF	chr13:85836020-85836170	Hela-S3	cervix:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
39	CTCF	chr13:85836000-85836150	GM12872	blood:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
40	CTCF	chr13:85836020-85836170	NHEK	skin:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
41	CTCF	chr13:85836040-85836190	GM12867	blood:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
42	CTCF	chr13:85835940-85836090	A549	lung:	n/a	n/a
43	CTCF	chr13:85819320-85819470	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr13:85836020-85836170	HPAF	blood vessel:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
45	CTCF	chr13:85836020-85836170	HBMEC	blood vessel:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
46	CTCF	chr13:85952000-85952150	HMEC	breast:	n/a	n/a
47	CTCF	chr13:85836020-85836170	WI-38	lung:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
48	CTCF	chr13:85836000-85836150	GM12875	blood:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
49	CTCF	chr13:85836040-85836190	GM12868	blood:	n/a	chr13:85836090-85836103 chr13:85836094-85836103
50	CTCF	chr13:85836040-85836190	HEK293	kidney:	n/a	chr13:85836090-85836103 chr13:85836094-85836103

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:85937861-85937911	GM12878	blood:	n/a
2	chr13:85937788-85937838	SK-N-MC	brain:	n/a
3	chr13:85915140-85915190	H1-hESC	embryonic stem cell:	embryo
4	chr13:85937730-85937780	SK-N-MC	brain:	n/a
5	chr13:85937788-85937838	HCF	heart:	n/a
6	chr13:85937788-85937838	HPAEpiC	pulmonary alveolar:	n/a
7	chr13:85779237-85779287	HIPEpiC	eye:	n/a
8	chr13:85937957-85938007	HRPEpiC	eye:	n/a
9	chr13:85779237-85779287	AoSMC	blood vessel:	n/a
10	chr13:85937730-85937780	MCF10A-Er-Src	breast:	n/a
11	chr13:85937518-85937568	HCT-116	colon:	n/a
12	chr13:85937957-85938007	RPTEC	kidney:	n/a
13	chr13:85915140-85915190	GM12878	blood:	n/a
14	chr13:85915140-85915190	K562	blood:	n/a
15	chr13:85937730-85937780	Caco-2	colon:	n/a
16	chr13:85779237-85779287	AG04449	skin:	fetal
17	chr13:85937518-85937568	AoSMC	blood vessel:	n/a
18	chr13:85937788-85937838	NHDF-neo	bronchial:	n/a
19	chr13:85937926-85937976	HRE	kidney:	n/a
20	chr13:85937926-85937976	Hepatocyte	liver:	n/a
21	chr13:85937730-85937780	SKMC	muscle:	n/a
22	chr13:85937861-85937911	HepG2	liver:	n/a
23	chr13:85937926-85937976	U87	brain:	n/a
24	chr13:85937730-85937780	A549	lung:	n/a
25	chr13:85937957-85938007	U87	brain:	n/a
26	chr13:85937926-85937976	IMR90	lung:	fetal
27	chr13:85937926-85937976	BJ	skin:	n/a
28	chr13:85937957-85938007	GM06990	blood:	n/a
29	chr13:85915140-85915190	Jurkat	blood:	n/a
30	chr13:85937518-85937568	AG09319	gingival:	n/a
31	chr13:85937957-85938007	HCPEpiC	choroid plexus:	n/a
32	chr13:85937730-85937780	Hela-S3	cervix:	n/a
33	chr13:85937730-85937780	GM12878	blood:	n/a
34	chr13:85779237-85779287	AG10803	skin:	n/a
35	chr13:85937518-85937568	PANC-1	pancreas:	n/a
36	chr13:85915140-85915190	HPAEpiC	pulmonary alveolar:	n/a
37	chr13:85915140-85915190	MCF-7	breast:	n/a
38	chr13:85937730-85937780	SK-N-SH_RA	brain:	n/a
39	chr13:85937926-85937976	Caco-2	colon:	n/a
40	chr13:85779237-85779287	Jurkat	blood:	n/a
41	chr13:85779237-85779287	BE2_C	brain:	n/a
42	chr13:85915140-85915190	AoSMC	blood vessel:	n/a
43	chr13:85937926-85937976	HL-60	blood:	n/a
44	chr13:85937926-85937976	PrEC	prostate:	n/a
45	chr13:85937926-85937976	AG04449	skin:	fetal
46	chr13:85779237-85779287	Caco-2	colon:	n/a
47	chr13:85937518-85937568	GM12891	blood:	n/a
48	chr13:85937518-85937568	H1-hESC	embryonic stem cell:	embryo
49	chr13:85937730-85937780	NHBE	bronchial:	n/a
50	chr13:85937861-85937911	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:85919914..85922732-chr13:85924658..85927029,2	K562	blood:
2	chr13:85815432..85817346-chr13:85817790..85819847,2	MCF-7	breast:
3	chr13:85784908..85787619-chr13:85787804..85790756,2	MCF-7	breast:
4	chr12:102083101..102085803-chr13:85724711..85727561,2	MCF-7	breast:
5	chr13:85784908..85787619-chr13:85787804..85790756,2	MCF-7	breast:
6	chr13:85815432..85817346-chr13:85817790..85819847,2	MCF-7	breast:
7	chr13:85919914..85922732-chr13:85924658..85927029,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-2	chr13:85742321-85742439	XLOC_010680
2	lnc-SLITRK5-11	chr13:85937738-85938230	NONHSAT034564
3	lnc-SLITRK6-2	chr13:85741303-85741462	XLOC_010680
4	lnc-SLITRK6-2	chr13:85743219-85743317	XLOC_010680
5	lnc-SLITRK6-3	chr13:85722163-85722284	XLOC_010679
6	lnc-SLITRK5-11	chr13:85937736-85938230	ENSG00000226317.2
7	lnc-SLITRK5-11	chr13:85937736-85938230	XLOC_010460
8	lnc-SLITRK6-3	chr13:85718789-85719009	XLOC_010679
9	lnc-SLITRK5-11	chr13:85937981-85938230	XLOC_010460
10	lnc-SLITRK6-3	chr13:85722163-85722284	XLOC_010679

Variant related genes	Relation type
LINC00351	TF binding region
LINC00351	CpG island
LIMK1	miRNA target sites
LIMD1	miRNA target sites
PDE3B	miRNA target sites
LIMD2	miRNA target sites

Extended variants
information (count: 3007 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3007 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60118858	chr13:85718458-85718459	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34064605	chr13:85718459-85718460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147644256	chr13:85718482-85718483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551889051	chr13:85718551-85718552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532057335	chr13:85718613-85718614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548423539	chr13:85718616-85718617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190533632	chr13:85718620-85718621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567657942	chr13:85718631-85718632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35638773	chr13:85718646-85718647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374001817	chr13:85718647-85718648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554290943	chr13:85718649-85718650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs386380025	chr13:85718652-85718653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58729493	chr13:85718654-85718655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199819680	chr13:85718655-85718656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200902842	chr13:85718657-85718658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201687755	chr13:85718658-85718659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs199865686	chr13:85718660-85718661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200834672	chr13:85718661-85718662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140451670	chr13:85718665-85718666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201500639	chr13:85718666-85718667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200083583	chr13:85718667-85718668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539779623	chr13:85718725-85718726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371283300	chr13:85718752-85718753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182365855	chr13:85718773-85718774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571244302	chr13:85718787-85718788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531349784	chr13:85718801-85718802	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs9575787	chr13:85718853-85718854	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs575439654	chr13:85718855-85718856	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs536349900	chr13:85718863-85718864	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs554843916	chr13:85718890-85718891	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs9575788	chr13:85718901-85718902	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540522629	chr13:85718922-85718923	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs536588904	chr13:85718972-85718973	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs34846449	chr13:85718977-85718978	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs558541511	chr13:85719040-85719041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140578166	chr13:85719051-85719052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9575789	chr13:85719061-85719062	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs185503258	chr13:85719112-85719113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200813123	chr13:85719134-85719135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372975196	chr13:85719137-85719138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562519752	chr13:85719139-85719140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111393308	chr13:85719150-85719151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs180705965	chr13:85719161-85719162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541883729	chr13:85719181-85719182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115469136	chr13:85719189-85719190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527855466	chr13:85719203-85719204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376198865	chr13:85719228-85719229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112216242	chr13:85719233-85719234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9593989	chr13:85719235-85719236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185764636	chr13:85719239-85719240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	19490664	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:85716800-85722000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr13:85719600-85721000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr13:85721000-85722000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr13:85722000-85722400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr13:85722000-85722400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr13:85722000-85722600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr13:85722000-85722600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr13:85722200-85722400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr13:85733600-85733800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr13:85741200-85741400	Enhancers	Fetal Lung	lung
11	chr13:85741600-85742600	Weak transcription	Fetal Lung	lung
12	chr13:85742600-85743000	Enhancers	Fetal Lung	lung
13	chr13:85743000-85743200	Weak transcription	Fetal Lung	lung
14	chr13:85743200-85743600	Enhancers	Fetal Lung	lung
15	chr13:85759800-85760800	Enhancers	Fetal Lung	lung
16	chr13:85760800-85761000	Flanking Active TSS	Fetal Lung	lung
17	chr13:85761000-85761200	Active TSS	Fetal Lung	lung
18	chr13:85761200-85761400	Flanking Active TSS	Fetal Lung	lung
19	chr13:85769000-85769400	Enhancers	Stomach Mucosa	stomach
20	chr13:85769400-85771000	Weak transcription	Stomach Mucosa	stomach
21	chr13:85771000-85771200	Active TSS	Stomach Mucosa	stomach
22	chr13:85771200-85771600	Weak transcription	Stomach Mucosa	stomach
23	chr13:85771400-85771800	Enhancers	HUVEC	blood vessel
24	chr13:85771600-85772200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr13:85771600-85772200	Enhancers	Stomach Mucosa	stomach
26	chr13:85778800-85779200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr13:85797600-85798000	Enhancers	Fetal Stomach	stomach
28	chr13:85797800-85798600	Enhancers	Fetal Heart	heart
29	chr13:85797800-85798800	Active TSS	Stomach Smooth Muscle	stomach
30	chr13:85798000-85798600	Enhancers	A549	lung
31	chr13:85798000-85798800	Enhancers	Fetal Lung	lung
32	chr13:85798000-85804200	Weak transcription	Fetal Stomach	stomach
33	chr13:85798800-85803600	Weak transcription	Fetal Lung	lung
34	chr13:85803600-85804200	Enhancers	Fetal Lung	lung
35	chr13:85804200-85804600	Weak transcription	Fetal Lung	lung
36	chr13:85804200-85805000	Enhancers	Fetal Stomach	stomach
37	chr13:85804600-85804800	Enhancers	Fetal Lung	lung
38	chr13:85804600-85805000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr13:85804800-85805200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr13:85804800-85805200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr13:85804800-85805200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr13:85804800-85805200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr13:85804800-85805200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr13:85804800-85805200	Active TSS	Brain Anterior Caudate	brain
45	chr13:85804800-85805200	Active TSS	Brain Substantia Nigra	brain
46	chr13:85804800-85805200	Active TSS	Fetal Kidney	kidney
47	chr13:85804800-85805200	Flanking Active TSS	Fetal Lung	lung
48	chr13:85804800-85805200	Enhancers	NHLF	lung
49	chr13:85805000-85805200	Enhancers	Brain Cingulate Gyrus	brain
50	chr13:85805000-85805200	Enhancers	Brain Inferior Temporal Lobe	brain

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